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The Journal of Neuroscience, October 1, 1998, 18(19):7739-7749

Amino Acid Residues that Control pH Modulation of Transport-Associated Current in Mammalian Serotonin Transporters

Yongwei Cao, Ming Li, Sela Mager, and Henry A. Lester

Division of Biology, California Institute of Technology, Pasadena, California 91125

    ABSTRACT
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References

The rat and human serotonin transporters (rSERT and hSERT, respectively) were expressed in Xenopus oocytes and studied using site-directed mutagenesis, electrophysiological recordings, and [3H]5-HT uptake measurements. rSERT, but not hSERT, displayed increased transport-associated current at low pH. Chimeras and point mutations showed that, of the 52 nonidentical residues, a single residue at position 490 (threonine in rSERT and lysine in hSERT) governs this difference. Furthermore, potentiation required the glutamate residue at position 493. Cysteine substitution and alkylation experiments showed that residue 493 is extracellular. Cysteine at 493 increased, whereas aspartate decreased, the net charge movement per transported 5-HT molecule. The mutations at this region did not significantly affect other aspects of SERT function, including agonist-independent leakage current, voltage-dependent transient current, and H+ current. This region may therefore be part of an external gate required for rSERT function. The data and analyses show that, in the absence of detailed structural information, a gate-lumen-gate scheme is useful for interpreting results from mutations that alter functional properties of neurotransmitter transporters.

Key words: 5-HT; Xenopus oocyte; protons; channels; electrophysiology; sodium

    INTRODUCTION
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References

The mammalian 5-HT transporter (SERT) plays an important role in terminating serotonergic transmission throughout the CNS and in peripheral tissues (Amara and Kuhar, 1993), constitutes a target for antidepressants and drugs of abuse (Rudnick and Clark, 1993), and displays variations in expression that are correlated with personality (Lesch et al., 1996) and with prevalence of affective disorders (Collier et al., 1996). cDNA cloning data show that vertebrate (Blakely et al., 1991; Hoffman et al., 1991; Lesch et al., 1993; Ramamoorthy et al., 1993) and invertebrate (Corey et al., 1994; Demchyshyn et al., 1994) SERT proteins belong to a family of related Na+, Cl--coupled neurotransmitter transporters that display overall similarities in the function as well as individual differences in the nature and stoichiometry of cotransported ions, rate of transport, and associated electrophysiological properties (Lester et al., 1994, 1996).

Recent experiments have uncovered four distinct conducting states of rSERT (Mager et al., 1994; Cao et al., 1997). (1) Classical stoichiometric data for SERT predict no net charge movement for each 5-HT molecule (see Fig. 9) (Rudnick and Clark, 1993). Yet electrophysiological recordings from oocytes expressing rSERT revealed current associated with 5-HT uptake (Mager et al., 1994). Previous studies showed that acidic pH increases this transport-associated current in rSERT; the EC50 for this effect is 7.8 µM H+, pH 5.1, and the Hill coefficient is 1.1, suggesting the involvement of a single acidic side chain. However, pH has no effect on 5-HT uptake (except at extreme pH), indicating that pH may affect this conducting state without affecting 5-HT binding and transport (Cao et al., 1997). Several other neurotransmitter transporters also display "excess" transport-associated current (Lester et al., 1996; Sonders and Amara, 1996; Galli et al., 1997). (2) There is a Na+ leakage current in the absence of 5-HT (Mager et al., 1994). High-resolution patch recordings revealed that the transport-associated current and the leakage current arise from unitary events that resemble single-channel openings, but the single-channel events that underlie the transport-associated current occur at a frequency of only one per ~750 transported 5-HT molecules (Lin et al., 1996). (3) There is a voltage-dependent transient current (Mager et al., 1994). (4) There is an additional current at low pH, probably carried by protons (Cao et al., 1997).

In this study, we have sought and found mutations that modify the first of these currents and its relationship to 5-HT transport. We find that the pH dependence of the transport-associated current differs between human (hSERT) and rat (rSERT) transporters. Previous experiments have successfully exploited chimeras between homologous transporters within the Na, Cl superfamily that specifically transport different substrates (Buck and Amara, 1994, 1995; Giros et al., 1994), and chimeras between the orthologous hSERT and rSERT transporters were used to localize a region distal to amino acid 532 that governs species preferences for the binding of imipramine and D-amphetamine (Barker et al., 1994). We have also exploited hSERT-rSERT chimeras. Analysis of point mutations then led to the conclusion that the set of residues governing this difference lies in an extracellular portion of the protein and may participate in an external gating process of the transporter.

    MATERIALS AND METHODS
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References

Plasmid DNAs, site-directed mutagenesis, and mRNA synthesis. The rSERT cDNA (Hoffman et al., 1991) was used in the expression vector pAMV-PA (Nowak et al., 1998) as described (Lin et al., 1996). The hSERT cDNA was isolated by Dr. Beth J. Hoffman (National Institute of Mental Health). The rSERT cDNA fragment was radiolabeled by random priming and used to isolate a 4.5 kb cDNA clone corresponding to a partial cDNA of the hSERT from a human raphe cDNA library (B. J. Hoffman, personal communication) constructed in pCDSP6T7 (Usdin et al., 1991). The 5' end of the coding region was isolated (B. J. Hoffman, personal communication) by rapid amplification of cDNA ends (Frohman et al., 1988) from human raphe poly(A+) RNA followed by PCR using two gene-specific 22-nt oligomers [upstream (sense), 5'-TTG GGA TCC TTG GCA GAT GGA C-3'; downstream (antisense), 5'-GCT GGT CCA GGG CAG CTG GTC C-3']. A complete cDNA was constructed by ligation of a BamHI/SstI digest of this PCR product to an SstI/EcoRV digest of the 3' end of the cDNA in pSP73 (New England Biolabs, Beverly, MA; http://www.neb.com). The sequence of the complete cDNA was verified by double-stranded sequencing. The cDNA insert was excised by digestion with SmaI and XbaI and transferred into the EcoRV and XbaI sites of a modified pAMV-PA vector (the AMV sequence was removed).

The C109A rSERT mutant was provided by Dr. Gary Rudnick (Yale University School of Medicine) (Chen et al., 1997a) and was also transferred into the pAMV-PA vector. Site-directed mutagenesis was performed using a PCR method (Higuchi, 1990). PCR products were subcloned into pAMV-PA, and the presence of the intended mutation was confirmed by sequencing. Plasmid DNAs were prepared using the Qiagen (Hilden, Germany; http://www.qiagen.com) miniprep kit and were linearized by NotI digestion. RNA was synthesized in vitro using the Ambion (Austin, TX; http://www.ambion.com) transcription kit.

Sequence alignments were performed using LaserGene software (DNASTAR, Madison, WI; http://www.dnastar.com). For the alignments of the short stretch (see Fig. 1C), a total of 65 Na+, Cl--dependent neurotransmitter transporters and orphan transporters was selected from the GenBank database. A candidate sequence (the human sequence when available) was then selected from each cluster and was realigned.

Oocyte expression. Stage V and VI oocytes were isolated and injected with ~20 ng of mRNA in 30-50 nl of water. Injected oocytes were then incubated 3-7 d at 19°C for translation (Quick and Lester, 1994).

Electrophysiology. Voltage-clamp experiments were performed using the two-electrode technique (Mager et al., 1994). Data acquisition and analysis were performed using the pCLAMP programs (Axon Instruments, Foster City, CA; http://www.axonet.com). Normal Na+ Ringer's solution contained 100 mM NaCl, 2 mM KCl, 1 mM MgCl2, 5 mM HEPES, and 5 mM MES. Solution pH was adjusted with NaOH or HCl to obtain pH 7.4 or 5.5 as indicated in the text. For cation substitution experiments, NaCl was replaced by equimolar N-methyl-D-glucamine (NMDG) chloride. Solution changes were made with electrically operated valves (Auto-Mate Scientific, San Francisco, CA). All recordings were performed at room temperature (21-22°C). Tracings in the figures represent similar traces recorded from at least three oocytes in each of two or three batches. A Fourier transform algorithm was used to suppress 60 Hz interference in some traces (see Fig. 3).

Sulfhydryl modification by methanethiosulfonate derivatives. Methanethiosulfonate-ethylammonium (MTSEA) and MTS-ethylsulfonate (MTSES) (Toronto Research Chemical Company, Toronto, Canada) were used for irreversible, covalent modification of cysteine residues. After an initial electrophysiological recording, oocytes were removed from the voltage-clamp chamber and incubated in Na+ Ringer's solution containing 0.5 mM MTSEA or 2 mM MTSES for 10 min. After incubation, the oocytes were washed and voltage-clamped a second time; these recordings were compared with the preincubation records to assess the effects of sulfhydryl modification.

MTS compounds were prepared as 1.0 M solutions in H2O and kept at -80°C. These stock solutions were diluted in the appropriate buffer solution at room temperature just before exposure to the oocyte.

5-HT uptake. 5-HT uptake was usually measured by a 3 min incubation in 300 µl of uptake solution containing 1 µM [3H]5-HT. Oocytes were washed once with the uptake solution before uptake began and three times after uptake ended. Oocytes were then solubilized in 2% SDS. The [3H]5-HT uptake was determined by liquid scintillation counting.

To determine 5-HT uptake during voltage clamp, we placed the oocyte in the recording chamber and held the membrane potential at -40 mV. The solution flow was then stopped, and [3H]5-HT was added with gentle stirring to a final concentration of 1 µM. Current induced by 5-HT was simultaneously recorded on a chart recorder. After 1 min, the recording chamber was perfused with Ringer's solution for 1 min.

    RESULTS
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References

Figure 1, A and B, presents the primary amino acid sequence and putative membrane topology of rSERT, which was used for most of our experiments, and of the human homolog hSERT (Blakely et al., 1991; Hoffman et al., 1991; Lesch et al., 1993; Ramamoorthy et al., 1993). Regions of special interest are marked. Sequence comparisons between rSERT and hSERT show that the two proteins have a high degree of similarity, with 52 different residues spanning a total of 630 amino acids (Fig. 1A).


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  		Figure 1.   Annotated amino acid sequences for rSERT and related transporters. A, Alignment between rSERT and hSERT (GenBank accession numbers X63253 and L05568, respectively). Putative membrane topology is indicated by the blue (intracellular), white (transmembrane, N terminal near the intracellular face), pink (extracellular), and gray (transmembrane, N terminal near the extracellular face) regions. Residues in rSERT are shown in dark blue letters; residues in hSERT (shown below rSERT in black) are dashed where identical to those in rSERT and shown explicitly where the two sequences differ, but for simplicity, differences are not shown for the N- and C-terminal intracellular regions (22 and 4 differences, respectively). Positions of conserved restriction enzyme sites that were used for chimera construction are marked by the enzyme name. Residues in which mutations have been studied in the present experiments are marked by down-arrow . Numbers mark the positions in which mutations were characterized (Figure legend continues)in previous studies: 1, C109 (Chen et al., 1997a); 2, I172, Y176, and I179 (Chen et al., 1997b); 3, N177 (Lin et al., 1996); and 4, S545 (Sur et al., 1997). The C109A mutant was used for some of the experiments in this paper (see Figs. 6, 7). TM, Transmembrane. B, Summary of the membrane topology shown in A. C, Alignments for 19 transporters, including ~44 residues in the putative extracellular region studied in this paper, flanking the E493 region of rSERT. Initially, a total of 65 Na+, Cl--dependent neurotransmitter transporters and orphan transporters was selected from the GenBank database. A candidate sequence (the human sequence if possible) was then selected from each cluster and was realigned. The rSERT residues mutated in this study are shown by down-arrow .

Acidic pH potentiates transport-associated current markedly in rSERT but not in hSERT

We reported previously that acidic pH significantly increased the transport-associated current in oocytes expressing rSERT (Cao et al., 1997). Figure 2 recapitulates this finding. In these experiments (see also the experiments described in Figs. 4-6 below), the pH-dependent enhancement of the transport-associated current was analyzed by comparing the transport-induced currents in individual oocytes at pH 7.4 with those at pH 5.5. This tactic presumably eliminates distortions from variations in expression level among the various constructs. In contrast, for hSERT expressed in oocytes, the transport-associated current was increased only slightly (20% in the trace in Fig. 2, right) and actually decreased in other experiments. For the batch of oocytes that yielded our most complete set of comparative data, transport-associated current for rSERT and hSERT at -40 mV increased to 399 ± 33% and decreased to 63 ± 1% (mean ± SEM; five oocytes), respectively, of the value at pH 7.4 when external pH was lowered to 5.5. 


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  		Figure 2.   Effects of acidic pH on transport-associated current in wild-type (WT) rSERT and hSERT. Note that pH 5.5 solution produces an additional inward current in the absence of 5-HT in both transporters (Cao et al., 1997). However, only in rSERT the pH 5.5 solution also increases the transport-associated current during 5-HT application. The holding potential was -40 mV. The base solution was normal Na+ Ringer's solution, pH 7.4. Applications of acidic Na+ Ringer's solution, pH 5.5, and 5-HT (3 µM) are indicated by horizontal bars.

Most measurements were made at a holding potential of -40 mV for consistency with our previous study (Cao et al., 1997), but in Figure 3, we analyze the voltage dependence of the transport-associated current at low pH. For both rSERT and hSERT, the transport-associated current at pH 5.5 increased at more negative potentials and displayed no clear reversal at positive potentials. This current-voltage relation is similar to that for the measurements at pH 7.4 (Mager et al., 1994), but the larger size of the current at pH 5.5 for rSERT allowed more accurate measurements. (We note that oocytes expressing hSERT generally displayed larger transport-associated currents than did those expressing rSERT, so that the enhanced current for rSERT was only twice as large as that for hSERT, even though the fractional enhancement at pH 5.5 was approximately four times larger for rSERT than for hSERT. We have not systematically explored the basis for the differing transport-associated currents, but the difference has persisted with two series of mRNA syntheses and with three oocyte batches.) At all membrane potentials between -20 and -100 mV, pH 5.5 enhanced the transport-induced current for rSERT several fold, but there was little enhancement or a decrease for hSERT. Other electrophysiological properties of hSERT, such as the presence of leakage current, H+ current, and transient current, did not differ significantly from those of rSERT (data not shown). Thus, this difference in the fractional enhancement of the transport-associated current by low pH constitutes a specific and limited electrophysiological distinction between rSERT and hSERT.


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  		Figure 3.   Voltage dependence of the transport-associated current at pH 5.5. A, Data for a representative oocyte expressing rSERT. Row 1, Voltage-clamp traces in the absence of 5-HT, pH 5.5. The membrane potential was held at -40 mV and jumped to test potentials at 10 mV increments between +40 mV and -100 mV for 100 msec. Row 2, Traces for the same voltage-clamp protocol applied 3 min later in the presence of 5-HT (3 µM), pH 5.5. Row 3, Subtraction revealing the 5-HT-induced current at pH 5.5. Note that the subtracted traces are displayed at a higher gain. B, Data for a representative oocyte expressing hSERT, with voltage-clamp protocols and subtraction described in A. The oscillations in the final epoch of row 3 are an artifact of the algorithm that suppressed 60 Hz interference earlier in the traces. C, The transport-associated current at pH 5.5 plotted versus membrane potential. The current was averaged over the final 30 msec of the test pulse. Data are mean ± SEM for five rSERT and four hSERT oocytes.

The different residues at position 490 are responsible for the different pH sensitivities of rSERT and hSERT

We constructed chimeric rSERT-hSERT proteins by swapping corresponding cDNA segments generated by restriction enzyme digestion at several conserved sites (SacI, BglII, and BamHI; see Fig. 1A). Measurements on oocytes expressing these chimeric transporters showed that transport-associated current was present in all four chimeras tested, but marked potentiation by pH 5.5 was seen only in chimeras containing the C-terminal 155 residues or more of the rSERT sequence (Fig. 4). Evidently this electrophysiological difference can be localized to a part of the transporter molecule consisting of the C-terminal 155 residues.


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  		Figure 4.   Localization of a region responsible for pH dependence of the transport-associated current. Experiments similar to those of Figure 2 were performed on chimeric rSERT-hSERT transporters. The constructs used restriction sites for SacI, BglII, and BamHI. For locations of each restriction enzyme site, see Figure 1. Note that all the data are consistent with the interpretation that pH 5.5 enhances the transport-associated currents in transporters containing C-terminal sequences from rSERT. The BamHI construct contains the fewest rSERT residues (155) and indicates that the sequences governing pH 5.5 enhancement are located in the C-terminal 155 residues.

We next asked whether the electrophysiological difference can be localized to a specific residue. In these 155 positions at the C terminal, rSERT and hSERT differ by 12 amino acid residues (Fig. 1A; four differences are not shown explicitly in the intracellular C terminal). We therefore began to mutate these residues individually. We first chose residues at positions 483 (rS483F; typical trace shown in Fig. 5A), 490 (rT490K; Fig. 5B), and 572 (rH572Y; Fig. 5C), because these residues are (1) polar and (2) thought to be in extracellular or transmembrane portions of the protein and thus more likely to respond to extracellular pH changes. Each of the three mutants was functional in oocytes, but only rT490K (Fig. 5B) showed a dramatically decreased low-pH potentiation of the transport-associated current. To verify that position 490 governs the difference in pH sensitivity between rSERT and hSERT, we made a reverse mutant in which K490 in hSERT was mutated to threonine (hK490T; Fig. 5D). This reverse mutation conferred an rSERT-like pH sensitivity on hSERT; the transport-associated current was now significantly increased by acidic pH.


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  		Figure 5.   Effects of acidic pH on transport-associated current from the point mutants rS483F (A), rT490K (B), rH572Y (C), hK490T (D), E493Q (E), and E494Q (F) and the double point mutant E493Q-E494Q (G). Recording conditions are described in the legend to Figure 2.

Protonation at E493 is mainly responsible for low-pH potentiation of transport-associated current

Previous results showed that the H+ potentiation of the transport-associated current displays a typical Michaelis-Menten relationship with an EC50 of 7.8 µM H+, pH 5.1, and a Hill coefficient of 1.1, indicating that a single amino acid with pKa ~ 5.1 might be responsible for low-pH potentiation (Cao et al., 1997). Threonine at position 490 is unlikely to be a candidate because its free-solution pKa is ~9.1. However, there are two consecutive glutamate residues (pKa ~ 4.7) at positions 493 and 494, just downstream of T490 (Fig. 1A). We suspected that protonation of one or both of these glutamate residues might actually be responsible for low-pH potentiation. To test this hypothesis, we mutated E493 and E494 in rSERT to glutamine and expressed the mutated transporters in oocytes. Results showed that a single mutation at 493 only (E493Q) still allowed low-pH potentiation but at a reduced level (approximately twofold vs fourfold for WT rSERT at pH 5.5; Fig. 5E). Mutation at 494 only (E494Q) displayed low-pH potentiation equal to that of WT rSERT (fourfold at pH 5.5; Fig. 5F). However, a double mutation at both 493 and 494 (E493Q-E494Q) almost completely abolished low-pH potentiation (Fig. 5G). These results suggest that E493 is mainly responsible for the low-pH potentiation. In the absence of E493, E494 partially fills the same role and allows for a moderate level of potentiation. However, potentiation also requires the absence of a positively charged residue at position 490, as though a lysine-glutamate salt bridge prevents protonation of the glutamate; and hSERT but not rSERT contains the lysine at position 490.

E493 is exposed to the extracellular solution

On the basis of standard topology models (Fig. 1A,B), E493 is located in the extracellular loop between the 9th and the 10th transmembrane segments. To verify the hypothesis of extracellular localization, we mutated E493 to cysteine and tested whether the mutated protein became sensitive to the externally applied cysteine-modifying reagents MTSEA and MTSES. Because WT rSERT is already sensitive to externally applied cysteine reagents, we chose the cysteine reagent-insensitive mutant C109A as our control transporter for this series of experiments (Chen et al., 1997a). Confirming the work of Chen et al. (1997a), we found that this mutant (denoted by the number 1 in Fig. 1A) functioned similarly to WT rSERT except for its reduced sensitivity to cysteine reagents (Chen et al., 1997a). Like WT rSERT, C109A showed an approximately fourfold increase in transport-associated current at pH 5.5 (Fig. 6A). As expected, incubation of C109A-expressing oocytes in MTSEA (0.5 mM) or MTSES (2 mM) for 10 min did not change the amplitude of the transport-associated current (Fig. 6C). The E493C mutant constructed on the C109A background (i.e., C109A-E493C double mutant) showed reduced low-pH potentiation of transport-associated current (two- to threefold at pH 5.5) (Fig. 6B). This result is expected from the data on the E493Q mutant (Fig. 5E). Importantly, the E493C mutant became sensitive to both MTSEA and MTSES (Fig. 6D). These results suggest that E493 is exposed to the extracellular solution.


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  		Figure 6.   Comparisons between transport-associated current in C109A and C109A-E493C. A, B, Effects of acidic pH on transport-associated current in typical traces from C109A (A) and C109A-E493C (B). Recording conditions are described in the legend to Figure 2. C, D, Effects of cysteine-modifying reagents MTSEA and MTSES on transport-associated current from C109A (C) and C109A-E493C (D). Transport-associated currents were recorded both before and after MTS-reagent treatments and were normalized to the current recorded before treatment. Error bars represent the SD in measurements from three oocytes.

E493C increases, and E493D decreases, the net charge movement per 5-HT molecule

Our previous results showed that acidic pH (in the range of 5.5 to 6.5 compared with pH 7.5) increases transport-associated current but does not change 5-HT uptake (Cao et al., 1997), indicating that H+ could increase the ionic flux for each 5-HT molecule further. To test whether this is also the case for the C109A-E493C mutant, we performed [3H]5-HT uptake experiments under voltage-clamp conditions so that [3H]5-HT uptake and total ionic flux could be measured simultaneously. We found that the E493C mutant transported 5.5-fold more charges per 5-HT molecule (ratio of 126 ± 21 charges per 5-HT; n = 3) than did the control C109A (21 ± 5 charges per 5-HT; n = 3) (Fig. 7A). Similar results were found with the E493Q mutant (data not shown). The E493C mutation did not change the amplitude of the leakage current or the Na+ dependence of 5-HT uptake (Fig. 7B). The transport-associated current depended on [5-HT] with similar EC50 values (0.3 ± 0.1 and 0.4 ± 0.1 µM; n = 3) and Hill coefficients (1.4 ± 0.2 and 1.3 ± 0.1) for C109A-E493C and the control C109A, respectively (Fig. 7C). The EC50 for Na+ was not significantly changed (data not shown). The hyperpolarization-induced transient current found in WT rSERT (Mager et al., 1994) was also present in C109A-E493C, although with reduced amplitude (Fig. 7D). As we expected from the data on WT SERT, this transient current was blocked by 5-HT (Fig. 7D). Thus, the most significant changes produced by the E493C mutation were (1) reduced pH sensitivity of transport-associated current and (2) increased net charge movement per 5-HT uptake.


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  		Figure 7.   Functional effects of the E493C mutation. A, Comparison of C109A and C109A-E493C on the ratio of net charge movement to net 5-HT uptake. Error bars represent the SD in measurements from three oocytes. B, Comparison of C109A-E493C and a control (C109A) on the Na+ dependence of 5-HT uptake. NMDG was used as a substitute for Na+. Error bars represent the SD in measurements from six oocytes. C, Dose-response relationship for the transport-associated current. Data were fit by nonlinear regression to the Hill equation. D, Voltage-dependent transient current in the C109A-E493C mutant and inhibition of this current by 5-HT. Current traces recorded in the presence (+) and absence (-) of 5-HT (3 µM) are superimposed. The voltage protocol is shown at the top.

Sequence alignment of the known Na+, Cl--coupled neurotransmitter transporters and some orphan transporters reveals that the negatively charged residue at position 493 of rSERT-hSERT is highly conserved, perhaps even in two orphan transporters from procaryotes (Fig. 1C). However, only mammalian 5-HT transporters have glutamate at this position; in most other transporters, this residue is aspartate. To test functional differences between glutamate and aspartate at this position, we constructed the E493D mutant in rSERT and expressed it in Xenopus oocytes. The E493D mutant displayed H+ leakage current (Fig. 8A) and transient current (Fig. 8B); the amplitudes of these two currents were similar to those of WT, suggesting a similar expression level. However, to our surprise, the E493D mutant displayed a much smaller transport-associated current of <5 nA at pH 7.4 (Fig. 8A) compared with the current of 10-20 nA normally seen with WT rSERT. Furthermore, the transport-associated current was no longer potentiated by acidic pH. 5-HT may even slightly inhibit the H+ leakage current (Fig. 8A). To test whether the E493D mutation also affects the charge per 5-HT ratio, we measured [3H]5-HT uptake under voltage-clamp conditions. As shown in Figure 8C, the charge per 5-HT ratio decreased by ~50% in E493D (8.1 ± 2.7 for E493D vs 17.2 ± 4.8 for WT; n = 3), indicating that there is less uncoupled charge movement per 5-HT molecule transported.


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  		Figure 8.   Characterization of the E493D mutant. A, Effect of acidic pH on transport-associated current. Recording conditions are described in the legend to Figure 2. B, Transient current in E493D and inhibition of this current by 5-HT. Current traces recorded in the presence and absence of 5-HT (3 µM) are superimposed. The voltage protocol is the same as that shown in Figure 7D. C, Comparison of E493D and WT on the ratio of net charge movement to net 5-HT uptake. Error bars represent the SD in measurements from three oocytes.

    DISCUSSION
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References

The mutations near position 490 described here produce specific and subtle functional anomalies, encouraging us to assume that the overall structure of SERT remains unchanged. The mutations change the transport-associated current, its dependence on pH, and the number of charges transported per 5-HT. But these mutations do not change the dose-response relation for 5-HT, the leakage current, or the voltage-dependent transient current. Although WT rSERT and WT hSERT differ in the binding of tricyclic antidepressants and of D-amphetamine, these differences are governed by residues downstream of position 532 rather than by positions 490 and 493 studied here (Barker et al., 1994).

The gate-lumen-gate model

We interpret our experiments in terms of a model for neurotransmitter transporter function in which the transport protein contains a channel-like lumen flanked by intracellular and extracellular gates (Fig. 9). These gates open and close individually and sequentially in response to the binding of transported substrates, with resulting changes in compartmentalization that form the essence of coupled transport (Lester et al., 1994, 1996). Although other conceptual models have been advanced (Su et al., 1996), the gate-lumen-gate scheme is useful if the external gate, the lumen, and the internal gate can be localized at the level of primary amino acid sequence (and ultimately at the atomic scale in three dimensions).


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  		Figure 9.   Schematic diagram of the transport cycle for SERT. Six numbered states are enclosed within an oval; arrowheads on the oval denote the direction of normal progression through the transport cycle. Fully coupled stoichiometry applies within the oval; one 5-HT molecule is transported into the cell along with a single Na+ ion and a single Cl- ion (states 6, 1, 2, and 3). A single K+ ion leaves (states 5 and 6). The external gate is labeled in red when open; the internal gate is labeled in blue when open. When 5-HT, Na+, and Cl- bind within the lumen, the external gate closes, and the internal gate opens (state 1 right-arrow state 2). This changes the compartmentalization of the three substrates, which accounts for their coupled flux. When K+ then binds within the lumen, the internal gate closes, and the external gate opens, accounting for the obligatory role of K+ (state 4 right-arrow state 5). Outside the oval is the state (2*) corresponding to the uncoupled transport-associated current. We hypothesize that this uncoupled transport-associated current represents a violation of the alternating-access rules; both gates are open simultaneously. Retaining the convention from the ion channel literature, we describe this conducting state by an *. The red arrows indicate probabilities, not formal rate constants; E493Q, E493C, and low pH increase the probability of state 2*, whereas E493D decreases this probability.

We want to state that the scheme of Figure 9 has some heuristic value but that it omits some relevant data on the order and cooperativity of substrate binding (Rudnick and Clark, 1993) and that it has no known relation to structural features on the atomic scale. The illustration shows six numbered states enclosed within an oval; arrowheads on the oval denote the direction of normal progression through the transport cycle. Within the oval, the accepted substrate stoichiometry prevails; one 5-HT molecule is transported into the cell along with a single Na+ ion and a single Cl- ion. A single K+ ion leaves. When 5-HT, Na+, and Cl- bind within the lumen, the external gate closes, and the internal gate opens. This changes the compartmentalization of the three substrates, which accounts for their coupled flux. When K+ then binds within the lumen, the internal gate closes, and the external gate opens, accounting for the obligatory role of K+.

Outside the oval is the uncoupled transport-associated current that we have studied and manipulated in these experiments. We hypothesize that this uncoupled current represents a violation of the alternating-access rules; both gates are open simultaneously (Lester et al., 1996; Sonders and Amara, 1996). An analogous state 1* can be suggested for the leakage current; indeed, we have found mutations affecting that current as well, and these will be reported separately. We do not believe that these currents are obligatory steps in the transport cycle (Lin et al., 1996, but see Galli et al., 1996); however, we have suggested that the various currents represent important constraints on the mechanism of transport (Lester et al., 1996).

The external gate may be near position 490

Position 490 and nearby residues are good candidates for partial involvement in external gating. We know that the region is extracellular, because the present data show that the 493C mutant is accessible to extracellular cysteine reagents. Mutations in this region change the pH sensitivity of the transport-associated current. The mutation could either change the conductance or affect the gating process (changing the open probability). However, the first possibility is unlikely because (1) E493 is located in an extracellular loop and is thus unlikely to line the permeation pathway and (2) the amplitude of the leakage current is not affected by this mutation. We thus favor the second possibility, that either the E493C mutation, the E493Q mutation, or low pH increase the open probability of the external gate. We schematize this influence (Fig. 9) by the red arrows connecting state 2 with the conducting state 2*, in which the external gate is abnormally open, whereas the internal gate is normally open.

Although the amino acid residue difference at position 490 is responsible for the different pH sensitivities of hSERT and rSERT, E493 in rSERT might be the actual residue that is protonated to cause increased transport-associated current. The positively charged lysine at 490 in hSERT would be one turn away from E493 in an alpha -helix. This lysine might prevent a proton from gaining access to E493 and thus abolish the low-pH potentiation. More specifically, the lysine might form a salt bridge with E493, stabilizing E493 in the charged form and thus stabilizing hSERT in a state equivalent to that of rSERT at higher pH. The requirement for glutamate is very strict; even the conservative substitution of aspartate abolishes the potentiation. Striking differences in coupling and pH dependence are caused by glutamate versus aspartate, in some cases because of salt bridges with lysine, in two other ion-coupled transporters: the Escherichia coli lactose permease (Sahin-Toth and Kaback, 1993) and the vesicular monoamine transporter (Merickel et al., 1997).

Several other neurotransmitter transporters tested to date have not revealed the low-pH potentiation of the transport-associated current (Cao et al., 1997). There are two possible bases for this unique behavior. (1) SERT is unusual because it is not electrogenic. For the GABA transporter GAT1, the transport-associated current is tightly coupled to the transport cycle; that is, the transport-associated current is explained by the stoichiometry of the events that occur within the oval of Figure 9 (Kavanaugh et al., 1992). The transport-associated current for SERT may arise instead from fortuitous operation of the gates, as described above. (2) Most other neurotransmitter transporters have aspartate at the position that aligns with 493 (Fig. 1C). Our results show that this residue abolishes the low-pH potentiation of rSERT and also reduces the transport-associated current at neutral pH (Fig. 8). An interesting question is whether the increased transport-associated current, governed in part by glutamate at position 493, has a physiological role either via the resulting depolarization or via the accumulation of internal Na+. Related roles have been suggested for the Cl- conductance associated with glutamate transporters (Sonders and Amara, 1996).

Progress in other studies

The S545A mutation in TM11 (marked as number 4 in Fig. 1A) decreases the Na+ specificity of transport (Sur et al., 1997). In external NMDG Ringer's solution, S545A shows no detectable transport. Compared with WT, S545A displays an increased EC50 for 5-HT and a reduced cooperativity for Na+ binding (Sur et al., 1997). The results with S545A suggested to Sur et al. (1997) that S545 is a component of the external gate and participates in initial Na+ binding. The gates are likely to comprise several portions of the transporter, in addition to the region suggested by our own studies.

There has also been progress in localizing the lumen. A mutation at G177 in TM3 (one of the mutations noted by number 2 in Fig. 1A) increases single-channel conductance (Lin et al., 1996). Cysteine residues introduced into TM3 are accessible to alkylating reagents at several positions, and the periodicity suggests an alpha -helical structure (also noted as number 2 in Fig. 1A) (Chen et al., 1997b), suggesting that TM3 may comprise part of the lumen. Results to date therefore suggest that the gate-lumen-gate scheme provides one possible theoretical framework, and perhaps a preliminary structural framework, for explaining SERT function.

    FOOTNOTES

Received June 23, 1998; accepted July 14, 1998.

This work was supported by Grant DA-09121 from the National Institute on Drug Abuse and Grant NS-11756 from the National Institute of Neurological Disorders and Stroke, by a National Institutes of Health National Research Service Award to Y.C., and by a National Alliance for Research on Schizophrenia and Depression fellowship to S.M. We thank B. J. Hoffman and G. Rudnick for providing cDNAs.

Correspondence should be addressed to Dr. Henry A. Lester, Division of Biology 156-29, California Institute of Technology, Pasadena, CA 91125.

Dr. Cao's present address: Monsanto Company, Mail Code CV-BRG, St. Louis, MO 63198;

Dr. Mager's present address: Department of Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7545.

    REFERENCES
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References

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